HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281716Generated: November 1, 2026
4-(2-Chloroethyl)morpholine → HCID 18422108, compound
https://huagongshe.com/reaction/1281716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(2-Chloroethyl)morpholine | HCID 76727 | — |
| Reactant | HCID 18422129 | HCID 18422129 | — |
| Product | HCID 18422108 | HCID 18422108 | 41% |
Reaction Steps
Using an analogous procedure to that described in Example 7 except that the reaction mixture was heated to 70° C. rather than 40° C., N-[3-(3-hydroxybenzamido)-4-methylphenyl]quinoline-6-carboxamide was reacted with 2-morpholinoethyl chloride to give the title compound in 41% yield, m.p. 216-217° C.; NMR Spectrum: (DMSOd6) 2.21 (s, 3H), 2.47 (m, 4H), 2.73 (t, 2H), 3.59 (t, 4H), 4.18 (t, 4H), 7.17 (m, 1H), 7.24 (d, 1H), 7.42 (t, 1H), 7.54 (s, 2H), 7,61 (m, 2H), 7.87 (s, 1H), 8.15 (d, 1H), 8.23 (m, 1H), 8.52 (m, 1H), 8.61 (s, 1H), 9.0 (d, 1H), 9.9 (s, 1H), 10.49 (s, 1H); Mass Spectrum: M+H+ 511.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06455520B1 |
|---|
| Source dataset | uspto-grants-2002_09 |
|---|
| ORD ID | ord-0faee0fac12f4d59a7197fe8ddea6c76 |
|---|
| Source note | uspto-grants-2002_09 |
|---|